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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253103Generated: October 29, 2026

Water → 1-Acetyl-5-(cyclohexylmethyl)piperidine-3-carboxylic acid

https://huagongshe.com/reaction/253103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantDichloromethaneHCID 6344—
ReactantEthyl 1-acetyl-5-(cyclohexylmethyl)piperidine-3-carboxylateHCID 66844834—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1-Acetyl-5-(cyclohexylmethyl)piperidine-3-carboxylic acidHCID 66844752—

Reaction Steps

LiOH (2 N, 500 μL) was added to a solution of ethyl 1-acetyl-5-(cyclohexylmethyl)piperidine-3-carboxylate (180 mL, 0.61 mmol) in MeOH (1 mL) and THF (5 mL). After being maintained for two hours, the reaction was poured into a mixture of CH2Cl2 (25 mL) and H2O (10 mL). The layers were separated and the aqueous layer was extracted with CH2Cl2 (10 mL). The aqueous layer was acidified to pH 1 with 1N HCl and extracted with CH2Cl2 (3×20 mL). The combined organic layers were sequentially washed with H2O (10 mL) and brine before being dried over Na2SO4. Concentration under reduced pressure provided the title compound as a colorless oil. MS m/z: 268.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872009B2
Source datasetuspto-grants-2011_01
ORD IDord-6965c2739f154d7097754183e47a9b59
Source noteuspto-grants-2011_01